EP0359377A1 - Dérivés de 1,4-dihydropyridine - Google Patents

Dérivés de 1,4-dihydropyridine Download PDF

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Publication number
EP0359377A1
EP0359377A1 EP89307578A EP89307578A EP0359377A1 EP 0359377 A1 EP0359377 A1 EP 0359377A1 EP 89307578 A EP89307578 A EP 89307578A EP 89307578 A EP89307578 A EP 89307578A EP 0359377 A1 EP0359377 A1 EP 0359377A1
Authority
EP
European Patent Office
Prior art keywords
group
dihydropyridine
compounds
dihydro
compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP89307578A
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German (de)
English (en)
Other versions
EP0359377B1 (fr
Inventor
Kenichi Suzuki
Haruaki Inada
Akira Kiue
Tetsuro Sano
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nikken Chemicals Co Ltd
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Nikken Chemicals Co Ltd
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Filing date
Publication date
Priority claimed from JP18671188A external-priority patent/JP2640245B2/ja
Priority claimed from JP5982889A external-priority patent/JP2678786B2/ja
Application filed by Nikken Chemicals Co Ltd filed Critical Nikken Chemicals Co Ltd
Publication of EP0359377A1 publication Critical patent/EP0359377A1/fr
Application granted granted Critical
Publication of EP0359377B1 publication Critical patent/EP0359377B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings

Definitions

  • the present invention relates to novel 1,4-dihydropyridine derivatives having pharmacological activity, more particularly to 1.4-dihydropyridine derivatives useful in the therapy for tumors.
  • U.S. Patent 4293700 discloses that a 1,4-dihydropyridine compound having no substituents at the 4- position has a metastasis inhibitory effect on some tumors.
  • U.S. Patent 4690935 discloses antitumor and anti-tumor metastasis agents comprising 1,4-dihydropyridine, such as nifedipine or nimodipine, as the active ingredient.
  • EP-A-221382 discloses a method of treating malignant tumors by using a combination of a platinum coordination compound and a compound such as nifedipine or nimodipine
  • EP-A-0270926 discloses that compounds having condensed heterocyles with a special structure bonded to the 4-position of 1,4-dihydropyridine potentiate a sensitivity of multi-drug resistant tumor cells.
  • Japanese Unexamined Patent Publication (Kokai) Nos. 64-31780 and 64-31781 disclose that the compounds represented by the below- mentioned formula (I), wherein R 2 is replaced by an alkyloxy group and n is an integer of 2 to 4, remarkably increase the sensitivity of tumor cells having an acquired resistance.
  • the inventions disclosed in above U.S. Patent 4690935 and EP-A-221382 use calcium channel blockers as antitumor drugs or use platinum coordination compounds in combination with antitumor drugs, and have a drawback in that the side effects thereof sometimes limit their practical use. More specifically, the calcium channel blockers used in the above prior art all have a potent hypotensive action (blood pressure lowering action), and are drugs capable of revealing actions for the cardio-vascular system, even in small amount, and therefore have a drawback in that the effect of inconvenient actions on the cardio-vascular system, such as marked hypotension, cannot be avoided when they are used in the large amounts necessary for antitumor action.
  • a 1,4-dihydropyridine derivative having the formula (I): wherein R, represented a 2-(5,6-dihydro-p-dioxinyl) 2-(5,6-dihydro-1,4-dithiinyl) or 2-(3-methyl-5,6-dihydro-1.4-dithiinyl) group provided that when R, is a 2-(5,6-dihydro-p-dioxinyl) group, R 2 is a pyridyl group which may be substituted with one methyl group or ethyl group and n is an integer of 1 to 4; and when R, is a 2-(5,6-dihydro-1,4-dithiinyl) or 2-(3-methyl-5,6-dihydro-1,4-dithiinyl) group, R 2 is a pyridyl group and n is 1 or 2.
  • one having a particularly conspicuous drug sensitivity potentiating action may be a compound wherein R 1 is 2-(5,6-dihydro-p-dioxinyl) group, R 2 is a pyridyl group or a pyridyl group substituted with one methyl group or ethyl group, and n is an integer of 1 to 3, or a compound wherein R, is 2-(5,6-dihydro-1,4-dithiinyl) group or 2-(3-methyl-5,6-dihydro-1,4-dithiinyl) group, R 2 is a pyridyl group, and n is 1.
  • All of the 1,4-dihydropyridine derivatives represented by the above formula (I) can be prepared by utilizing reactions well known in the art and utilized for the preparation of 1,4-dihydropyridines.
  • they can be prepared by allowing 2-formyl-p-dioxene, 2-formyl-1,4-dithiene or 2-formyl-3-methyl-1,4-dithiene to react with S-aminocrotonic ester and acetoacetic ester in the presence or absence of an organic solvent by heating or by heating under reflux (method A), or by allowing 2-formyl-p-dioxene, 2-formyl-1,4-dithiene or 2-formyl-3-methyl-1,4-dithiene to react with acetoacetic ester and ammonia water in the presence or absence of an organic solvent by heating, preferably under reflux (method B).
  • the reactions used in these preparation methods are basically the same as the reactions used in the prior art for the preparation of 1,4-dihydropyridine compounds (e.g., the reactions used in the methods described in Japanese Patent Publication (Kokoku) Nos. 46-40625, 56-37225, and Japanese Unexamined Patent Publication (Kokai) No. 60-214786). Accordingly, the 1,4-dihydropyridine derivatives of the present invention can be also prepared by utilizing other known reactions in addition to the above methods.
  • the starting compounds to be used in the above preparation methods are all known compounds, and are readily available or can be easily prepared by those skilled in the art. Namely, acetoacetic ester and p-aminoctoronic ester are both compounds conventionally used as starting materials for the preparation of 1,4-dihydropyridine compounds, and are commercially readily available, or can be readily synthesized. Further, 2-formyl-p-dioxene can be prepared by the method described in M. S. Shostakovskii; Izvest. Akad. Nauk. S. S. S. R. Otdel. Khim. Nauk., 1685, (1961).
  • 2-formyi-1,4-dithiene or 2-formyl-3-methyl-1,4-dithiene can be prepared by using 1,4-dithiene or 2-methyl-1,4-dithiene as the starting material and reacting dimethylformamide and phosphorus oxychloride therewith, followed by a hydrolysis of the obtained product; specifically, they can be prepared by the method described in Japanese Unexamined Patent Publication (Kokai) No. 64-31781.
  • the reaction product formed according to the above method i.e., the 1.4-dihydropyridine derivative represented by the formula (I)
  • the reaction mixture can be separated from the reaction mixture and punfied in a conventional manner, for example, by extraction with a solvent by chromatography or by crystallization.
  • a 4.00 g (0.035 mole) amount of 2-formyl-p-dioxene, 17.9 g (0.081 mole) of 3-(3-pyridyl)propyl acetoacetate and 15 ml of 28% ammonia water were dissolved in 25 ml of isopropyl alcohol and heated under reflux for 20 hours.
  • a 4.00 g (0.035 mole) amount of 2-formyl-p-dioxene 17.0 g (0.082 mole) of 2-(2-pyridyl)ethyl acetoacetate and 15 ml of 28% ammonia water were dissolved in 100 ml of isopropyl alcohol and heated under reflux for 48 hours. After cooling, the reaction mixture was concentrated, the residue was dissolved in ethyl acetate, and the impurities were removed by extraction with a small amount of water.
  • a 4.00 g (0.027 mole) amount of 2-formyl-1,4-dithiene, 11.4 g (0.059 mole) of 3-pyridylmethyl acetoacetate and 15 ml of 28% ammonia water were dissolved in 25 ml of isopropyl alcohol and heated under reflux for 20 hours. After cooling, the reaction mixture was concentrated, the residue was dissolved in ethyl acetate, and the impurities were removed by extraction with a small amount of water. The ethyl acetate layer was dried over anhydrous sodium sulfate and the solvent then concentrated.
  • VCR vincristine-resistant mouse leukemia
  • P388 / VCR vincristine-resistant mouse leukemia
  • the compounds of this invention and VCR were administered intraperitoneally once a day for 5 consecutive days, the animals were observed, and the survival days for respective animals were determined to obtain the survival ratio (T/C)% relative to the Control.
  • the potentiating effect of the antitumor agent (T/V)% was determined according to the formula shown below.
  • Verapamil was employed as the positive Control compound.
  • the compounds of this invention and the positive Control compound were suspended in a vehicle of 0.5% CMC-Na containing 0.1% Tween 80 and VCR was dissolved in sterilized physiological saline. The results are shown in Tables 1 to 4.
  • Compound 1 is the compound obtained in Example 1, Compound 2 that obtained in Example 2, Compound 3 that obtained in Example 3, Compound 4 that obtained in Example 4, and Compound 5 that obtained in Example 5.
  • VCR vincristine-resistant mouse leukemia
  • P388/VCR vincristine-resistant mouse leukemia
  • VCR vincristine-resistant mouse leukemia
  • P388/VCR vincristine-resistant mouse leukemia
  • the compounds of this invention were administered orally after the treatment described above, and VCR was administered as described above.
  • the progress thereof was observed and the survival days for respective animals were determined to obtain the survival ratio (T/C)% relative to the Control.
  • the antitumor agent potentiating effect (T/V)% was determined as described above.
  • Table 8(A) In the Table, Compound 8 is the compound obtained in Example 8.
  • Rat rectum (about 1.5 cm) was isolated and suspended in a Magnus tube.
  • a Locke solution was employed as the nutrient solution, and a contraction of the intestinum rectum was caused by changing the potassium (K) concentration of this solution from 5.6 mmol (mM) to 56.0 mM.
  • K potassium
  • This contraction was a contraction through a membrane dependent Ca-channel mediated contraction based on depolarization by a K concentration change.
  • the contraction was recorded by an FD-transducer and polygraph.
  • the compounds of the present invention were permitted to act 5 minutes before changing the K concentration, and simultaneously with changing the K concentration.
  • the compounds of the present invention and the positive Control compound were all dissolved in dimethyl sulfoxide (DMSO) and the concentrations in the nutrient solution were made 10- 8 and 10- 7 mole (M). A judgement was made 5 minutes after changing the K concentration, and the difference in contraction before the concentration change was indicated as an inhibition % value. Verapamil and nicardipine were employed as the positive control compound . The results are shown in Table 9. In the Table, the respective compounds have the same meanings as described in Example 11.
  • the systolic blood pressure was measured by using spontaneously hypertensive rats (SHR), which are a model of hypertension when examine the hypotensive activities of the compounds of the present invention and the positive Control compound.
  • SHR spontaneously hypertensive rats
  • the rats were warmed for 5 minutes in a warming box at 55 C, and their blood pressure then measured by a tail cuff plethysmograph.
  • the compounds of the present invention were administered singly and intraperitoneally at a dose of 100 mgikg and the positive Control compound was administered singly and intraperitoneally 'at a dose of 10 mg/kg.
  • the compounds of the present invention and the positive Control compound were administered in the same manner as described in Example 11. Blood pressure measurements were taken before administration and 60 minutes after administration. Nicardipine was employed as the positive Control compound. The results are shown in Table 10 and Table 11. In the Tables, the respective compounds have the same meanings as described in Example 11 and Example 12.
  • mice Male 6-week-old ICR mice were divided into groups of 2 to 5 mice per group. General signs were observed for 10 days after an intraperitoneal administration of compounds of the present invention, and the mortality rates were determined.
  • the drugs to be tested were administered in varying amounts of 250 to 2000 mg/kg to 5 or 7 groups (a geometrical series of ⁇ 2), at a dose volume of 10 ml/kg. The results are shown in Table 12. In the Table, the respective compounds have the same meanings as described above.
  • the 1,4-dihydropyridine derivative according to the present invention can be used in combination with an antitumor drug to potentiate the effect thereof.
  • This effect is particularly marked for clones having acquired a resistance to the antitumor drug.
  • P388/VCR cells which is a vincristine-resistant clone
  • substantially no life prolonging effect can be obtained by the administration of an antitumor drug alone, but a life prolonging effect can be clearly recognized upon the administration of the compound of the present invention in combination therewith (Fig. 1 to Fig. 8), and the mean survival days are clearly prolonged compared with a VCR single administration (potentiating effect 116 to 156%).
  • This life prolonging effect is conspicuous when compared in terms of the life prolonging ratio (T C %).
  • Compound 8 has an effect comparable to the prolonging effect when VCR is administered alone to P388/S which is a vincristine-sensitive clone (Table 8), thus completely overcoming the VCR resistance.
  • the compounds of the present invention have a very weak calcium channel blocking activity compared to many other 1,4-dihydropyridine compounds (Table 9), and very little side effects such as hypotension (Table 10 and Table 11). Further, the compounds of the present invention have an extremely low toxicity (Table 12). Therefore, the compounds of the present invention are useful for the therapy of tumors having an acquired resistance.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Hydrogenated Pyridines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
EP89307578A 1988-07-28 1989-07-25 Dérivés de 1,4-dihydropyridine Expired - Lifetime EP0359377B1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP18671188A JP2640245B2 (ja) 1988-07-28 1988-07-28 １，４−ジヒドロピリジン誘導体
JP186711/88 1988-07-28
JP5982889A JP2678786B2 (ja) 1989-03-14 1989-03-14 １，４―ジヒドロピリジン誘導体
JP59828/89 1989-03-14

Publications (2)

Publication Number Publication Date
EP0359377A1 true EP0359377A1 (fr) 1990-03-21
EP0359377B1 EP0359377B1 (fr) 1993-10-13

Family

ID=26400906

Family Applications (1)

Application Number Title Priority Date Filing Date
EP89307578A Expired - Lifetime EP0359377B1 (fr) 1988-07-28 1989-07-25 Dérivés de 1,4-dihydropyridine

Country Status (5)

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US (1) US4985558A (fr)
EP (1) EP0359377B1 (fr)
CA (1) CA1331613C (fr)
DE (1) DE68909873T2 (fr)
ES (1) ES2059767T3 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5389644A (en) * 1992-02-05 1995-02-14 Adir Et Compagnie 1,4-dihydropyridine compounds

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9119983D0 (en) * 1991-09-19 1991-11-06 Erba Carlo Spa Dihydropyridine derivatives useful in antitumor therapy
US7439052B2 (en) * 2000-06-29 2008-10-21 Lipid Sciences Method of making modified immunodeficiency virus particles
US6693099B2 (en) 2000-10-17 2004-02-17 The Procter & Gamble Company Substituted piperazine compounds optionally containing a quinolyl moiety for treating multidrug resistance
US6376514B1 (en) * 2000-10-17 2002-04-23 The Procter & Gamble Co. Substituted six-membered heterocyclic compounds useful for treating multidrug resistance and compositions and methods thereof
AU2002322284A1 (en) * 2001-06-25 2003-01-08 Lipid Sciences, Inc. Systems and methods using multiple solvents for the removal of lipids from fluids
US6991727B2 (en) * 2001-06-25 2006-01-31 Lipid Sciences, Inc. Hollow fiber contactor systems for removal of lipids from fluids

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2218644A1 (de) * 1972-04-18 1973-10-25 Bayer Ag Basische ester von 1,4-dihydropyridinen, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel
EP0087156A1 (fr) * 1982-02-23 1983-08-31 Nikken Chemicals Co., Ltd. Dérivés de 1,4-dihydropyridine et leur procédé de préparation
EP0118120A2 (fr) * 1983-03-04 1984-09-12 Nikken Chemicals Co., Ltd. Composé 1,4-dihydropyridine
EP0123850A2 (fr) * 1983-03-31 1984-11-07 The Board Of Governors Of Wayne State University Inhibition de la croissance de tumeurs et de la métastase avec des bloqueurs de canaux de calcium
EP0173204A2 (fr) * 1984-08-30 1986-03-05 Bayer Ag 1,4-Dihydropyridines, leur procédé de préparation et leur application comme médicaments
EP0270926A2 (fr) * 1986-11-26 1988-06-15 Kyorin Seiyaku Kabushiki Kaisha Agents favorisant l'activité de quelques agents antitumeurs et leurs méthodes de préparation

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU725406A1 (ru) * 1978-08-08 1981-07-30 Ордена Трудового Красного Знамениинститут Органического Синтеза Ah Латвий-Ской Ccp Эфиры диметил дигидропиридин диКАРбОНОВОй КиСлОТы,ОблАдАющиЕ АНТи-МЕТАСТАТичЕСКОй АКТиВНОСТью
US4906646A (en) * 1983-03-31 1990-03-06 Board Of Governors Of Wayne State University Method and composition for the treatment of tumors by administering a platinum coordination compound and a calcium channel blocker compound of the dihydropyridine class
JPH0692391B2 (ja) * 1987-07-17 1994-11-16 インステイテユト オルガニチエスコゴ シンテザ，アカデミヤ ナウク ラトビイスコイ エスエスエ−ル １，４−ジヒドロピリジン誘導体
JPH0692401B2 (ja) * 1987-07-17 1994-11-16 インステイテユト オルガニチエスコゴ シンテザ，アカデミヤ ナウク ラトビイスコイ エスエスエ−ル １，４−ジヒドロピリジン誘導体

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2218644A1 (de) * 1972-04-18 1973-10-25 Bayer Ag Basische ester von 1,4-dihydropyridinen, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel
EP0087156A1 (fr) * 1982-02-23 1983-08-31 Nikken Chemicals Co., Ltd. Dérivés de 1,4-dihydropyridine et leur procédé de préparation
EP0118120A2 (fr) * 1983-03-04 1984-09-12 Nikken Chemicals Co., Ltd. Composé 1,4-dihydropyridine
EP0123850A2 (fr) * 1983-03-31 1984-11-07 The Board Of Governors Of Wayne State University Inhibition de la croissance de tumeurs et de la métastase avec des bloqueurs de canaux de calcium
EP0173204A2 (fr) * 1984-08-30 1986-03-05 Bayer Ag 1,4-Dihydropyridines, leur procédé de préparation et leur application comme médicaments
EP0270926A2 (fr) * 1986-11-26 1988-06-15 Kyorin Seiyaku Kabushiki Kaisha Agents favorisant l'activité de quelques agents antitumeurs et leurs méthodes de préparation

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5389644A (en) * 1992-02-05 1995-02-14 Adir Et Compagnie 1,4-dihydropyridine compounds

Also Published As

Publication number Publication date
DE68909873T2 (de) 1994-02-10
DE68909873D1 (de) 1993-11-18
CA1331613C (fr) 1994-08-23
US4985558A (en) 1991-01-15
EP0359377B1 (fr) 1993-10-13
ES2059767T3 (es) 1994-11-16

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